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Welcome to GCSE Edexcel Science revision.

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Unit C B 5: Health, disease and the development of medicines.

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Health includes physical, mental and social well-being, not only the absence of disease.

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Problems in one area can affect the others.

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Communicable diseases are caused by pathogens and can spread between organisms.

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Non-communicable diseases are not passed from one person to another by infection.

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A pathogen is a disease-causing agent, such as a bacterium, virus, fungus or protist.

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Not all microorganisms cause disease.

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One disease can increase vulnerability to another.

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For example, H I V damages immune defences, so other infections can become harder to control.

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A correlation is a pattern linking two variables.

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It does not prove that one causes the other (causation).

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For example, income and life expectancy may be linked, but healthcare, nutrition and housing can also affect the pattern.

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Compare health data using suitable samples, rates or percentages.

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Look for other factors that could explain the pattern (confounding factors).

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An increased risk means something is more likely, not certain to happen.

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Many non-communicable diseases result from interacting genetic, environmental and lifestyle factors.

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Examples include cardiovascular disease, some cancers and some lung or liver diseases.

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Malnutrition means an unbalanced intake of nutrients or energy, including deficiencies and excesses.

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Lack of vitamin C can cause scurvy; excess energy intake can contribute to increased body fat.

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Diet and physical activity affect energy balance.

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Long-term energy intake exceeding energy expenditure can contribute to obesity, which is associated with increased risk of several diseases.

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Body mass index (B M I)  equals  mass in kilograms divided by (height in metres)squared.

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Square the height before dividing; convert centimetres to metres if needed.

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A hypothetical adult of mass seventy two kilograms and height one point eight metres has body mass index equal to seventy two divided by one point eight squared,

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which equals twenty two point two to one decimal place.

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In the conventional adult B M I classification commonly used in GCSE examples, 30 or above indicates obesity.

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B M I is a screening measure, not a diagnosis; it cannot distinguish muscle from fat, and children require age-related interpretation.

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Waist : hip ratio  equals  waist circumference divided by hip circumference.

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Use the same units: a waist of 80 centimetres and hips of 100 centimetres give a ratio of 0.80.

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B M I and waist : hip ratio can contribute to risk assessment, but do not capture every influence on health.

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Use the information supplied in an exam question rather than diagnosing an individual from one value.

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Alcohol misuse can damage the liver and contribute to cirrhosis, where healthy tissue is replaced by scar tissue.

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Alcohol is not the only possible cause of liver disease.

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Smoking increases cardiovascular risk by damaging blood vessels and contributing to plaque formation and clotting.

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Nicotine can raise heart rate and blood pressure; carbon monoxide reduces the blood’s oxygen-carrying capacity.

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Lifestyle-related disease affects individuals and families, healthcare services and wider society.

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Population effects depend on exposure, access to care and other factors; avoid assuming that a disease is solely a person’s fault.

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Cardiovascular disease affects the heart or blood vessels.

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In coronary heart disease, fatty deposits can narrow the coronary arteries supplying heart muscle.

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Reduced blood flow limits the supply of oxygen for aerobic respiration in heart muscle.

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A clot blocking a coronary artery can cause a heart attack.

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Lifestyle changes can reduce cardiovascular risk.

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Their benefits usually develop over time; they do not instantly remove an established arterial blockage.

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Medicines such as statins lower blood cholesterol and can reduce risk.

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They may require long-term use and can have side effects, so evaluate benefits and limitations.

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A stent is a small mesh tube inserted into a narrowed artery to help keep it open.

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Angioplasty widens the artery, and the stent supports the opening.

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A stent supports a widened passage; it does not remove every underlying risk factor.

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Coronary bypass surgery uses a blood vessel graft to make an alternative route around a narrowed or blocked artery, improving blood supply to heart muscle.

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Stents and bypass surgery can improve blood flow relatively quickly, but involve procedural risks and do not remove all underlying risk factors.

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Compare treatments using effectiveness, side effects, surgical risk, recovery, long-term care and cost.

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The most suitable treatment depends on the condition and the person.

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Bacteria are cells that can reproduce in suitable conditions.

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Some cause disease by damaging tissues or producing toxins; viruses reproduce inside host cells and can damage them.

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Cholera is caused by bacteria and can cause severe diarrhoea.

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It is commonly spread by water contaminated with infected faeces.

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Tuberculosis (TB) is caused by bacteria and can damage the lungs.

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Infectious material from a person with respiratory TB can spread through the air.

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Chalara ash dieback is caused by a fungus, Hymenoscyphus fraxineus.

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It causes leaf loss and bark lesions in ash trees; airborne fungal spores can spread infection.

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Athlete’s foot is a fungal infection that affects human skin, especially between the toes.

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Malaria is caused by Plasmodium protists and can damage blood and the liver.

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Mosquitoes act as vectors that carry the pathogen between people.

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H I V is a virus that damages immune-system cells.

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Untreated infection can lead to AIDS, leaving the body much less able to control other infections; effective treatment can prevent this progression.

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Chlamydia is a bacterial sexually transmitted infection (S T I).

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H I V can also be sexually transmitted, but it is caused by a virus, so the two pathogens are different types.

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A vector transports a pathogen between hosts.

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In malaria, the mosquito is the vector and the Plasmodium protist is the pathogen; they are not the same organism.

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Clean water supplies, sewage treatment and hygiene reduce faecal contamination and help prevent cholera transmission.

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Handwashing also reduces transfer of some pathogens to the mouth.

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Ventilation and appropriate infection-control measures reduce airborne transmission, including the spread of respiratory TB.

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Different transmission routes require different controls.

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For malaria, insecticide-treated mosquito nets, reducing breeding sites and controlling mosquitoes can reduce contact with the vector and interrupt transmission.

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Control measures for ash dieback aim to limit movement of infected material and follow plant-health guidance.

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Airborne spores make complete prevention difficult.

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S T I s such as chlamydia and H I V can spread through sexual contact involving infected fluids or tissues.

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Condoms reduce the risk of transmission; they do not guarantee protection against every S T I.

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Screening can identify infections, including those without obvious symptoms.

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Detection enables treatment and measures to reduce onward transmission; avoiding sexual contact prevents exposure by that route.

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Skin is a physical barrier that reduces entry of pathogens.

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Breaks in the skin can provide an entry route.

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Mucus traps particles and pathogens in the airways.

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Cilia move the mucus towards the throat, helping clear trapped material.

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Tears contain lysozyme, an enzyme that breaks down cell walls of some bacteria.

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This is a chemical defence, rather than a physical wall.

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Hydrochloric acid in the stomach creates acidic conditions that help destroy many swallowed pathogens.

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It is a chemical defence.

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Physical barriers and clearance work alongside chemical defences.

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Physical barriers reduce entry or remove pathogens; chemical defences use substances that damage them.

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These general defences do not target one particular antigen.

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Antigens are molecules, often on a pathogen’s surface, that can trigger a specific immune response.

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Different pathogens have different antigens.

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Lymphocytes are white blood cells involved in specific immune responses.

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Those that recognise a particular antigen multiply and produce antibodies with binding sites that match (are complementary to) that antigen.

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Antibodies are proteins that bind specifically to matching antigens.

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They can neutralise pathogens or toxins and help other immune cells remove pathogens; binding does not mean every pathogen is instantly destroyed.

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Other white blood cells, including phagocytes, can engulf and digest pathogens.

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Antibodies can help mark a pathogen for removal.

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The first exposure produces a primary immune response.

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There is a delay while the appropriate lymphocytes are activated and multiply.

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Some lymphocytes become memory cells and remain after the initial response.

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They enable a faster response if the same antigen is encountered again.

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The secondary response usually produces antibodies more rapidly and in greater quantities.

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Specificity means memory for one antigen does not automatically protect against every other pathogen.

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Vaccination introduces a safe form of an antigen, for example from an inactive pathogen or a harmless part of it.

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This stimulates an immune response without causing the disease the vaccine aims to prevent.

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The immune system produces specific antibodies and memory lymphocytes.

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Vaccination prepares the body for a later encounter; it does not simply supply a permanent stock of antibodies.

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On later exposure to the matching pathogen, memory cells enable a faster secondary response.

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The pathogen may be controlled before serious symptoms develop.

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Vaccine protection varies between pathogens, vaccines and people.

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Some vaccines require additional doses to build or maintain protection.

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A graph of antibody level against time can compare responses: the secondary response rises sooner and often reaches a higher level than the primary response.

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Interpret the axes and exposure times.

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Responses to the same antigen: schematic trend, not measured data.

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Antibiotics treat bacterial infections by killing bacteria or stopping their growth (inhibiting it).

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They target bacterial processes, such as making cell walls, that differ from processes in human cells.

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Antibiotics do not treat viral infections.

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Viruses use host-cell machinery and lack the bacterial structures or processes targeted by these medicines.

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Antibiotic-resistant bacteria survive a treatment that kills susceptible bacteria.

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Selection can make resistance more common as the survivors reproduce.

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Appropriate antibiotic use reduces unnecessary selection pressure.

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Pain-relieving medicines can relieve symptoms, but this does not mean they remove the pathogen.

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Medicine development starts by finding a substance that might have a useful effect.

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Researchers develop it into a form that can be given to a patient (a formulation) and investigate how it works.

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Before testing on humans, preclinical studies test a possible medicine on cells or tissues and, where appropriate, whole organisms.

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Researchers check its effects and toxicity (how harmful it is) and find out how it behaves in the body.

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Early clinical trials often use small numbers of healthy volunteers to study safety, side effects and suitable doses.

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Some medicines, such as certain cancer treatments, are first tested in patients instead.

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Later clinical trials include people with the condition and assess efficacy: how well the treatment works.

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Larger trials also give more information about side effects and comparisons with existing treatments.

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Studies move from preclinical tests to human trials, followed by review and monitoring.

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Random allocation helps make treatment and comparison groups similar.

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A placebo is a treatment without the tested active ingredient; some trials instead compare with an existing medicine.

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In a double-blind trial, participants and the relevant researchers assessing outcomes do not know which treatment each person receives.

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This helps reduce expectation and observer bias.

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Trials require informed consent, ethical review and monitoring.

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A placebo is not suitable if it would mean withholding essential effective treatment.

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Evaluate a medicine using efficacy, safety, appropriate dose and the quality of the evidence.

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A larger trial can detect effects missed by a small trial, but cannot prove a medicine has no risks.

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After approval, continued monitoring can identify rare or long-term side effects.

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Passing early tests is not a guarantee that every later study will be successful.

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That completes Health, disease and the development of medicines.

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Revisit the notes and test yourself on the revision website.
